Human Phenotype Ontology 
Grandparent Node:
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Abnormality of eye movement (HP:0000496)help
Parent Node:
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Abnormality of ocular smooth pursuit (HP:0000617)help
..Starting node
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Impaired smooth pursuit (HP:0007772)help
Term ID: 7772
Name: Impaired smooth pursuit
Synonym: Abnormal visual pursuit; Abnormality of visual tracking; Impairment of visual pursuit
Definition: An impairment of the ability to track objects with the ocular smooth pursuit system, a class of rather slow eye movements that minimizes retinal target motion.
Comments:
Reference: HP:0007772
Genes and Diseases:
 
       Child Nodes:
........expandImpaired horizontal smooth pursuit (HP:0001151) help
........expandAbsent smooth pursuit (HP:0007179) help

 Sister Nodes: 
..expandImpaired pursuit initiation and maintenance (HP:0007668) help
..expandJerky ocular pursuit movements (HP:0008003) help
..expandSaccadic smooth pursuit (HP:0001152) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007772HP:0007772Impaired smooth pursuit0ATXN10 CL E G H2581498761ORPHA19910549611150
HP:0007772HP:0007772Impaired smooth pursuit0ATXN10 CL E G H2581498761ORPHA110110549611150
HP:0007772HP:0007772Impaired smooth pursuit0ATXN8 CL E G H724066608768Spinocerebellar ataxia 8608768C1837454OMIM1232925613289
HP:0007772HP:0007772Impaired smooth pursuit0ATXN8OS CL E G H6315608768Spinocerebellar ataxia 8608768C1837454OMIM17610561603680
HP:0007772HP:0007772Impaired smooth pursuit0ATXN8OS CL E G H6315608768Spinocerebellar ataxia 8608768C1837454OMIM17210561603680
HP:0007772HP:0007772Impaired smooth pursuit0CACNA1A CL E G H773183086Spinocerebellar ataxia 6183086C0752124OMIM123261388601011
HP:0007772HP:0007772Impaired smooth pursuit0CACNA1A CL E G H773183086Spinocerebellar ataxia 6183086C0752124OMIM120471388601011
HP:0007772HP:0007772Impaired smooth pursuit0ELOVL4 CL E G H6785133190Erythrokeratodermia with ataxia133190C1851481OMIM121314415605512
HP:0007772HP:0007772Impaired smooth pursuit0ELOVL4 CL E G H6785133190Erythrokeratodermia with ataxia133190C1851481OMIM117814415605512
HP:0007772HP:0007772Impaired smooth pursuit0FGF14 CL E G H2259609307Spinocerebellar ataxia 27609307C1836383OMIM11873671601515
HP:0007772HP:0007772Impaired smooth pursuit0FGF14 CL E G H2259609307Spinocerebellar ataxia 27609307C1836383OMIM11903671601515
HP:0007772HP:0007772Impaired smooth pursuit0GNB1 CL E G H2782616973Mental retardation, autosomal dominant 42616973C4310774OMIM12504396139380
HP:0007772HP:0007772Impaired smooth pursuit0GNB1 CL E G H2782616973Mental retardation, autosomal dominant 42616973C4310774OMIM12174396139380
HP:0007772HP:0007772Impaired smooth pursuit0INPP5E CL E G H56623213300Joubert syndrome 1213300CN119531OMIM155921474613037
HP:0007772HP:0007772Impaired smooth pursuit0INPP5E CL E G H56623213300Joubert syndrome 1213300CN119531OMIM146621474613037
HP:0007772HP:0007772Impaired smooth pursuit0ITPR1 CL E G H3708606658Spinocerebellar ataxia 15606658C1847725OMIM19696180147265
HP:0007772HP:0007772Impaired smooth pursuit0ITPR1 CL E G H3708606658Spinocerebellar ataxia 15606658C1847725OMIM18956180147265
HP:0007772HP:0007772Impaired smooth pursuit0MAN2B1 CL E G H4125248500Deficiency of alpha-mannosidase248500C0024748OMIM17906826609458
HP:0007772HP:0007772Impaired smooth pursuit0MAN2B1 CL E G H4125248500Deficiency of alpha-mannosidase248500C0024748OMIM16536826609458
HP:0007772HP:0007772Impaired smooth pursuit0MRE11 CL E G H4361604391Ataxia-telangiectasia-like disorder 1604391C1858391OMIM112597230600814
HP:0007772HP:0007772Impaired smooth pursuit0MRE11 CL E G H4361604391Ataxia-telangiectasia-like disorder 1604391C1858391OMIM112587230600814
HP:0007772HP:0007772Impaired smooth pursuit0NOP56 CL E G H10528614153Spinocerebellar ataxia 36614153C3472711OMIM14415911614154
HP:0007772HP:0007772Impaired smooth pursuit0NOP56 CL E G H10528614153Spinocerebellar ataxia 36614153C3472711OMIM14315911614154
HP:0007772HP:0007772Impaired smooth pursuit0PEX10 CL E G H5192247815ORPHA14808851602859
HP:0007772HP:0007772Impaired smooth pursuit0PEX10 CL E G H5192247815ORPHA15788851602859
HP:0007772HP:0007772Impaired smooth pursuit0PEX10 CL E G H5192614871Peroxisome biogenesis disorder 6B614871C3553948OMIM15788851602859
HP:0007772HP:0007772Impaired smooth pursuit0PEX10 CL E G H5192614871Peroxisome biogenesis disorder 6B614871C3553948OMIM14808851602859
HP:0007772HP:0007772Impaired smooth pursuit0PLA2G6 CL E G H8398610217Neurodegeneration with brain iron accumulation 2b610217C1857747OMIM15139039603604
HP:0007772HP:0007772Impaired smooth pursuit0PLA2G6 CL E G H8398610217Neurodegeneration with brain iron accumulation 2b610217C1857747OMIM14319039603604
HP:0007772HP:0007772Impaired smooth pursuit0PRNP CL E G H5621137440Gerstmann-Straussler-Scheinker syndrome137440C0017495OMIM11469449176640
HP:0007772HP:0007772Impaired smooth pursuit0PRNP CL E G H5621137440Gerstmann-Straussler-Scheinker syndrome137440C0017495OMIM11319449176640
HP:0007772HP:0007772Impaired smooth pursuit0SACS CL E G H26278270550Spastic ataxia Charlevoix-Saguenay type270550C1849140OMIM1208810519604490
HP:0007772HP:0007772Impaired smooth pursuit0SACS CL E G H26278270550Spastic ataxia Charlevoix-Saguenay type270550C1849140OMIM1191410519604490
HP:0007772HP:0007772Impaired smooth pursuit0SPTBN2 CL E G H6712600224Spinocerebellar ataxia 5600224C0752123OMIM156911276604985
HP:0007772HP:0007772Impaired smooth pursuit0SPTBN2 CL E G H6712600224Spinocerebellar ataxia 5600224C0752123OMIM147811276604985
HP:0007772HP:0007772Impaired smooth pursuit0STT3A CL E G H3703370921ORPHA11936172601134
HP:0007772HP:0007772Impaired smooth pursuit0STT3A CL E G H3703370921ORPHA11756172601134
HP:0007772HP:0007772Impaired smooth pursuit0SYT14 CL E G H255928614229Spinocerebellar ataxia, autosomal recessive 11614229C3280226OMIM18423143610949
HP:0007772HP:0007772Impaired smooth pursuit0TMEM216 CL E G H51259608091Joubert syndrome 2608091C1842577OMIM116825018613277
HP:0007772HP:0007772Impaired smooth pursuit0TMEM216 CL E G H51259608091Joubert syndrome 2608091C1842577OMIM115125018613277
HP:0007772HP:0007772Impaired smooth pursuit0TSEN54 CL E G H283989277470Pontocerebellar hypoplasia type 2A277470C1848526OMIM126527561608755
HP:0007772HP:0007772Impaired smooth pursuit0TSEN54 CL E G H283989277470Pontocerebellar hypoplasia type 2A277470C1848526OMIM122027561608755
HP:0007772HP:0007772Impaired smooth pursuit0TULP1 CL E G H7287613843Leber congenital amaurosis 15613843C3151206OMIM131112423602280
HP:0007772HP:0007772Impaired smooth pursuit0TULP1 CL E G H7287613843Leber congenital amaurosis 15613843C3151206OMIM140712423602280
HP:0007772HP:0007179Absent smooth pursuit1ATXN10 CL E G H2581498761ORPHA19910549611150
HP:0007772HP:0001151Impaired horizontal smooth pursuit1ATXN10 CL E G H2581498761ORPHA110110549611150
HP:0007772HP:0001151Impaired horizontal smooth pursuit1ATXN10 CL E G H2581498761ORPHA19910549611150
HP:0007772HP:0007179Absent smooth pursuit1ATXN10 CL E G H2581498761ORPHA110110549611150
HP:0007772HP:0001151Impaired horizontal smooth pursuit1ATXN8 CL E G H724066608768Spinocerebellar ataxia 8608768C1837454OMIM1232925613289
HP:0007772HP:0007179Absent smooth pursuit1ATXN8 CL E G H724066608768Spinocerebellar ataxia 8608768C1837454OMIM1232925613289
HP:0007772HP:0001151Impaired horizontal smooth pursuit1ATXN8OS CL E G H6315608768Spinocerebellar ataxia 8608768C1837454OMIM17210561603680
HP:0007772HP:0007179Absent smooth pursuit1ATXN8OS CL E G H6315608768Spinocerebellar ataxia 8608768C1837454OMIM17610561603680
HP:0007772HP:0007179Absent smooth pursuit1ATXN8OS CL E G H6315608768Spinocerebellar ataxia 8608768C1837454OMIM17210561603680
HP:0007772HP:0001151Impaired horizontal smooth pursuit1ATXN8OS CL E G H6315608768Spinocerebellar ataxia 8608768C1837454OMIM17610561603680
HP:0007772HP:0001151Impaired horizontal smooth pursuit1CACNA1A CL E G H773183086Spinocerebellar ataxia 6183086C0752124OMIM123261388601011
HP:0007772HP:0001151Impaired horizontal smooth pursuit1CACNA1A CL E G H773183086Spinocerebellar ataxia 6183086C0752124OMIM120471388601011
HP:0007772HP:0007179Absent smooth pursuit1CACNA1A CL E G H773183086Spinocerebellar ataxia 6183086C0752124OMIM123261388601011
HP:0007772HP:0007179Absent smooth pursuit1CACNA1A CL E G H773183086Spinocerebellar ataxia 6183086C0752124OMIM120471388601011
HP:0007772HP:0001151Impaired horizontal smooth pursuit1ELOVL4 CL E G H6785133190Erythrokeratodermia with ataxia133190C1851481OMIM121314415605512
HP:0007772HP:0001151Impaired horizontal smooth pursuit1ELOVL4 CL E G H6785133190Erythrokeratodermia with ataxia133190C1851481OMIM117814415605512
HP:0007772HP:0007179Absent smooth pursuit1ELOVL4 CL E G H6785133190Erythrokeratodermia with ataxia133190C1851481OMIM121314415605512
HP:0007772HP:0007179Absent smooth pursuit1ELOVL4 CL E G H6785133190Erythrokeratodermia with ataxia133190C1851481OMIM117814415605512
HP:0007772HP:0007179Absent smooth pursuit1FGF14 CL E G H2259609307Spinocerebellar ataxia 27609307C1836383OMIM11873671601515
HP:0007772HP:0001151Impaired horizontal smooth pursuit1FGF14 CL E G H2259609307Spinocerebellar ataxia 27609307C1836383OMIM11903671601515
HP:0007772HP:0001151Impaired horizontal smooth pursuit1FGF14 CL E G H2259609307Spinocerebellar ataxia 27609307C1836383OMIM11873671601515
HP:0007772HP:0007179Absent smooth pursuit1FGF14 CL E G H2259609307Spinocerebellar ataxia 27609307C1836383OMIM11903671601515
HP:0007772HP:0001151Impaired horizontal smooth pursuit1GNB1 CL E G H2782616973Mental retardation, autosomal dominant 42616973C4310774OMIM12504396139380
HP:0007772HP:0001151Impaired horizontal smooth pursuit1GNB1 CL E G H2782616973Mental retardation, autosomal dominant 42616973C4310774OMIM12174396139380
HP:0007772HP:0007179Absent smooth pursuit1GNB1 CL E G H2782616973Mental retardation, autosomal dominant 42616973C4310774OMIM12504396139380
HP:0007772HP:0007179Absent smooth pursuit1GNB1 CL E G H2782616973Mental retardation, autosomal dominant 42616973C4310774OMIM12174396139380
HP:0007772HP:0007179Absent smooth pursuit1INPP5E CL E G H56623213300Joubert syndrome 1213300CN119531OMIM155921474613037
HP:0007772HP:0007179Absent smooth pursuit1INPP5E CL E G H56623213300Joubert syndrome 1213300CN119531OMIM146621474613037
HP:0007772HP:0001151Impaired horizontal smooth pursuit1INPP5E CL E G H56623213300Joubert syndrome 1213300CN119531OMIM155921474613037
HP:0007772HP:0001151Impaired horizontal smooth pursuit1INPP5E CL E G H56623213300Joubert syndrome 1213300CN119531OMIM146621474613037
HP:0007772HP:0007179Absent smooth pursuit1ITPR1 CL E G H3708606658Spinocerebellar ataxia 15606658C1847725OMIM19696180147265
HP:0007772HP:0007179Absent smooth pursuit1ITPR1 CL E G H3708606658Spinocerebellar ataxia 15606658C1847725OMIM18956180147265
HP:0007772HP:0001151Impaired horizontal smooth pursuit1ITPR1 CL E G H3708606658Spinocerebellar ataxia 15606658C1847725OMIM19696180147265
HP:0007772HP:0001151Impaired horizontal smooth pursuit1ITPR1 CL E G H3708606658Spinocerebellar ataxia 15606658C1847725OMIM18956180147265
HP:0007772HP:0001151Impaired horizontal smooth pursuit1MAN2B1 CL E G H4125248500Deficiency of alpha-mannosidase248500C0024748OMIM17906826609458
HP:0007772HP:0001151Impaired horizontal smooth pursuit1MAN2B1 CL E G H4125248500Deficiency of alpha-mannosidase248500C0024748OMIM16536826609458
HP:0007772HP:0007179Absent smooth pursuit1MAN2B1 CL E G H4125248500Deficiency of alpha-mannosidase248500C0024748OMIM17906826609458
HP:0007772HP:0007179Absent smooth pursuit1MAN2B1 CL E G H4125248500Deficiency of alpha-mannosidase248500C0024748OMIM16536826609458
HP:0007772HP:0001151Impaired horizontal smooth pursuit1MRE11 CL E G H4361604391Ataxia-telangiectasia-like disorder 1604391C1858391OMIM112597230600814
HP:0007772HP:0001151Impaired horizontal smooth pursuit1MRE11 CL E G H4361604391Ataxia-telangiectasia-like disorder 1604391C1858391OMIM112587230600814
HP:0007772HP:0007179Absent smooth pursuit1MRE11 CL E G H4361604391Ataxia-telangiectasia-like disorder 1604391C1858391OMIM112597230600814
HP:0007772HP:0007179Absent smooth pursuit1MRE11 CL E G H4361604391Ataxia-telangiectasia-like disorder 1604391C1858391OMIM112587230600814
HP:0007772HP:0001151Impaired horizontal smooth pursuit1NOP56 CL E G H10528614153Spinocerebellar ataxia 36614153C3472711OMIM14315911614154
HP:0007772HP:0007179Absent smooth pursuit1NOP56 CL E G H10528614153Spinocerebellar ataxia 36614153C3472711OMIM14415911614154
HP:0007772HP:0007179Absent smooth pursuit1NOP56 CL E G H10528614153Spinocerebellar ataxia 36614153C3472711OMIM14315911614154
HP:0007772HP:0001151Impaired horizontal smooth pursuit1NOP56 CL E G H10528614153Spinocerebellar ataxia 36614153C3472711OMIM14415911614154
HP:0007772HP:0007179Absent smooth pursuit1PEX10 CL E G H5192247815ORPHA14808851602859
HP:0007772HP:0001151Impaired horizontal smooth pursuit1PEX10 CL E G H5192247815ORPHA15788851602859
HP:0007772HP:0001151Impaired horizontal smooth pursuit1PEX10 CL E G H5192247815ORPHA14808851602859
HP:0007772HP:0007179Absent smooth pursuit1PEX10 CL E G H5192247815ORPHA15788851602859
HP:0007772HP:0007179Absent smooth pursuit1PEX10 CL E G H5192614871Peroxisome biogenesis disorder 6B614871C3553948OMIM15788851602859
HP:0007772HP:0007179Absent smooth pursuit1PEX10 CL E G H5192614871Peroxisome biogenesis disorder 6B614871C3553948OMIM14808851602859
HP:0007772HP:0001151Impaired horizontal smooth pursuit1PEX10 CL E G H5192614871Peroxisome biogenesis disorder 6B614871C3553948OMIM15788851602859
HP:0007772HP:0001151Impaired horizontal smooth pursuit1PEX10 CL E G H5192614871Peroxisome biogenesis disorder 6B614871C3553948OMIM14808851602859
HP:0007772HP:0001151Impaired horizontal smooth pursuit1PLA2G6 CL E G H8398610217Neurodegeneration with brain iron accumulation 2b610217C1857747OMIM14319039603604
HP:0007772HP:0007179Absent smooth pursuit1PLA2G6 CL E G H8398610217Neurodegeneration with brain iron accumulation 2b610217C1857747OMIM15139039603604
HP:0007772HP:0007179Absent smooth pursuit1PLA2G6 CL E G H8398610217Neurodegeneration with brain iron accumulation 2b610217C1857747OMIM14319039603604
HP:0007772HP:0001151Impaired horizontal smooth pursuit1PLA2G6 CL E G H8398610217Neurodegeneration with brain iron accumulation 2b610217C1857747OMIM15139039603604
HP:0007772HP:0007179Absent smooth pursuit1PRNP CL E G H5621137440Gerstmann-Straussler-Scheinker syndrome137440C0017495OMIM11469449176640
HP:0007772HP:0007179Absent smooth pursuit1PRNP CL E G H5621137440Gerstmann-Straussler-Scheinker syndrome137440C0017495OMIM11319449176640
HP:0007772HP:0001151Impaired horizontal smooth pursuit1PRNP CL E G H5621137440Gerstmann-Straussler-Scheinker syndrome137440C0017495OMIM11469449176640
HP:0007772HP:0001151Impaired horizontal smooth pursuit1PRNP CL E G H5621137440Gerstmann-Straussler-Scheinker syndrome137440C0017495OMIM11319449176640
HP:0007772HP:0007179Absent smooth pursuit1SACS CL E G H26278270550Spastic ataxia Charlevoix-Saguenay type270550C1849140OMIM1208810519604490
HP:0007772HP:0007179Absent smooth pursuit1SACS CL E G H26278270550Spastic ataxia Charlevoix-Saguenay type270550C1849140OMIM1191410519604490
HP:0007772HP:0001151Impaired horizontal smooth pursuit1SACS CL E G H26278270550Spastic ataxia Charlevoix-Saguenay type270550C1849140OMIM1208810519604490
HP:0007772HP:0001151Impaired horizontal smooth pursuit1SACS CL E G H26278270550Spastic ataxia Charlevoix-Saguenay type270550C1849140OMIM1191410519604490
HP:0007772HP:0007179Absent smooth pursuit1SPTBN2 CL E G H6712600224Spinocerebellar ataxia 5600224C0752123OMIM156911276604985
HP:0007772HP:0007179Absent smooth pursuit1SPTBN2 CL E G H6712600224Spinocerebellar ataxia 5600224C0752123OMIM147811276604985
HP:0007772HP:0001151Impaired horizontal smooth pursuit1SPTBN2 CL E G H6712600224Spinocerebellar ataxia 5600224C0752123OMIM156911276604985
HP:0007772HP:0001151Impaired horizontal smooth pursuit1SPTBN2 CL E G H6712600224Spinocerebellar ataxia 5600224C0752123OMIM147811276604985
HP:0007772HP:0001151Impaired horizontal smooth pursuit1STT3A CL E G H3703370921ORPHA11756172601134
HP:0007772HP:0007179Absent smooth pursuit1STT3A CL E G H3703370921ORPHA11936172601134
HP:0007772HP:0007179Absent smooth pursuit1STT3A CL E G H3703370921ORPHA11756172601134
HP:0007772HP:0001151Impaired horizontal smooth pursuit1STT3A CL E G H3703370921ORPHA11936172601134
HP:0007772HP:0007179Absent smooth pursuit1SYT14 CL E G H255928614229Spinocerebellar ataxia, autosomal recessive 11614229C3280226OMIM18423143610949
HP:0007772HP:0001151Impaired horizontal smooth pursuit1SYT14 CL E G H255928614229Spinocerebellar ataxia, autosomal recessive 11614229C3280226OMIM18423143610949
HP:0007772HP:0001151Impaired horizontal smooth pursuit1TMEM216 CL E G H51259608091Joubert syndrome 2608091C1842577OMIM116825018613277
HP:0007772HP:0001151Impaired horizontal smooth pursuit1TMEM216 CL E G H51259608091Joubert syndrome 2608091C1842577OMIM115125018613277
HP:0007772HP:0007179Absent smooth pursuit1TMEM216 CL E G H51259608091Joubert syndrome 2608091C1842577OMIM116825018613277
HP:0007772HP:0007179Absent smooth pursuit1TMEM216 CL E G H51259608091Joubert syndrome 2608091C1842577OMIM115125018613277
HP:0007772HP:0001151Impaired horizontal smooth pursuit1TSEN54 CL E G H283989277470Pontocerebellar hypoplasia type 2A277470C1848526OMIM126527561608755
HP:0007772HP:0001151Impaired horizontal smooth pursuit1TSEN54 CL E G H283989277470Pontocerebellar hypoplasia type 2A277470C1848526OMIM122027561608755
HP:0007772HP:0007179Absent smooth pursuit1TSEN54 CL E G H283989277470Pontocerebellar hypoplasia type 2A277470C1848526OMIM126527561608755
HP:0007772HP:0007179Absent smooth pursuit1TSEN54 CL E G H283989277470Pontocerebellar hypoplasia type 2A277470C1848526OMIM122027561608755
HP:0007772HP:0007179Absent smooth pursuit1TULP1 CL E G H7287613843Leber congenital amaurosis 15613843C3151206OMIM131112423602280
HP:0007772HP:0001151Impaired horizontal smooth pursuit1TULP1 CL E G H7287613843Leber congenital amaurosis 15613843C3151206OMIM140712423602280
HP:0007772HP:0001151Impaired horizontal smooth pursuit1TULP1 CL E G H7287613843Leber congenital amaurosis 15613843C3151206OMIM131112423602280
HP:0007772HP:0007179Absent smooth pursuit1TULP1 CL E G H7287613843Leber congenital amaurosis 15613843C3151206OMIM140712423602280
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007772HP:0007772Impaired smooth pursuit0ATXN8 CL E G H72406698760ORPHA0232925613289
HP:0007772HP:0007772Impaired smooth pursuit0ATXN8OS CL E G H631598760ORPHA07610561603680
HP:0007772HP:0007772Impaired smooth pursuit0ATXN8OS CL E G H631598760ORPHA07210561603680
HP:0007772HP:0007772Impaired smooth pursuit0GNB1 CL E G H2782488613ORPHA02174396139380
HP:0007772HP:0007772Impaired smooth pursuit0GNB1 CL E G H2782488613ORPHA02504396139380
HP:0007772HP:0007772Impaired smooth pursuit0KCND3 CL E G H375298772ORPHA02666239605411
HP:0007772HP:0007772Impaired smooth pursuit0KCND3 CL E G H375298772ORPHA02336239605411
HP:0007772HP:0001151Impaired horizontal smooth pursuit1ATXN8 CL E G H72406698760ORPHA0232925613289
HP:0007772HP:0007179Absent smooth pursuit1ATXN8 CL E G H72406698760ORPHA0232925613289
HP:0007772HP:0001151Impaired horizontal smooth pursuit1ATXN8OS CL E G H631598760ORPHA07210561603680
HP:0007772HP:0007179Absent smooth pursuit1ATXN8OS CL E G H631598760ORPHA07610561603680
HP:0007772HP:0007179Absent smooth pursuit1ATXN8OS CL E G H631598760ORPHA07210561603680
HP:0007772HP:0001151Impaired horizontal smooth pursuit1ATXN8OS CL E G H631598760ORPHA07610561603680
HP:0007772HP:0007179Absent smooth pursuit1GNB1 CL E G H2782488613ORPHA02174396139380
HP:0007772HP:0001151Impaired horizontal smooth pursuit1GNB1 CL E G H2782488613ORPHA02504396139380
HP:0007772HP:0001151Impaired horizontal smooth pursuit1GNB1 CL E G H2782488613ORPHA02174396139380
HP:0007772HP:0007179Absent smooth pursuit1GNB1 CL E G H2782488613ORPHA02504396139380
HP:0007772HP:0001151Impaired horizontal smooth pursuit1KCND3 CL E G H375298772ORPHA02336239605411
HP:0007772HP:0007179Absent smooth pursuit1KCND3 CL E G H375298772ORPHA02666239605411
HP:0007772HP:0007179Absent smooth pursuit1KCND3 CL E G H375298772ORPHA02336239605411
HP:0007772HP:0001151Impaired horizontal smooth pursuit1KCND3 CL E G H375298772ORPHA02666239605411


Genes (30) :ATXN1 ATXN10 ATXN2 ATXN3 ATXN8 ATXN8OS CACNA1A EEF2 ELOVL4 FGF14 GNB1 INPP5E ITPR1 KCND3 MAN2B1 MRE11 NOP56 PEX10 PLA2G6 POLR3B PRNP RARS SACS SPTBN2 STT3A STXBP1 SYT14 TMEM216 TSEN54 TULP1

Diseases (33) :98761 98760 608768 183086 133190 609307 488613 616973 213300 606658 98772 248500 604391 614153 247815 614871 610217 137440 270550 600224 370921 614229 608091 277470 613843 164400 183090 109150 101112 609306 614381 438114 612164
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.